陶氏病
神经退行性变
τ蛋白
高磷酸化
神经科学
疾病
病态的
痴呆
阿尔茨海默病
医学
生物信息学
生物
病理
细胞生物学
磷酸化
作者
Shibi Muralidar,Senthil Visaga Ambi,Saravanan Sekaran,Thirumalai Diraviyam,P. Balamurugan
标识
DOI:10.1016/j.ijbiomac.2020.07.327
摘要
Alzheimer's disease (AD) is a prevalently found tauopathy characterized by memory loss and cognitive insufficiency. AD is an age-related neurodegenerative disease with two major hallmarks which includes extracellular amyloid plaques made of amyloid-β (Aβ) and intracellular neurofibrillary tangles of hyperphosphorylated tau. With population aging worldwide, there is an indispensable need for treatment strategies that can potentially manage this developing dementia. Despite broad researches on targeting Aβ in the past two decades, research findings on Aβ targeted therapeutics failed to prove efficacy in the treatment of AD. Tau protein with its extensive pathological role in several neurodegenerative diseases can be considered as a promising target candidate for developing therapeutic interventions. The abnormal hyperphosphorylation of tau plays detrimental pathological functions which ultimately lead to neurodegeneration. This review will divulge the importance of tau in AD pathogenesis, the interplay of Aβ and tau, the pathological functions of tau, and potential therapeutic strategies for an effective management of neuronal disorders.
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